FHIR IG Statistics: ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set

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{
  "resourceType": "ValueSet",
  "id": "covid91-underlying-hemoglobinopathy-condition-value-set",
  "text": {
    "status": "generated",
    "div": "<!-- snip (see above) -->"
  },
  "url": "http://hl7.org/fhir/us/covid19library/ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set",
  "version": "1.0.0",
  "name": "COVID19UnderlyingHemoglobinopathyConditionVS",
  "title": "COVID-19 hemoglobinopathy underlying condition reference set",
  "status": "active",
  "date": "2022-07-25T12:22:40+00:00",
  "publisher": "HL7 International - Clinical Information Modeling Initiative",
  "contact": [
    {
      "name": "HL7 International - Clinical Information Modeling Initiative",
      "telecom": [
        {
          "system": "url",
          "value": "http://hl7.org/Special/committees/cimi"
        }
      ]
    },
    {
      "name": "Logica",
      "telecom": [
        {
          "system": "url",
          "value": "https://www.logicahealth.org/"
        }
      ]
    },
    {
      "name": "HL7",
      "telecom": [
        {
          "system": "url",
          "value": "https://www.hl7.org"
        }
      ]
    }
  ],
  "description": "A set of codes that describe underlying hemoglobinopathy conditions for COVID19",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "US",
          "display": "United States of America"
        }
      ]
    }
  ],
  "copyright": "This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement",
  "compose": {
    "include": [
      {
        "system": "http://snomed.info/sct",
        "concept": [
          {
            "code": "68913001",
            "display": "Alpha thalassemia (disorder)"
          },
          {
            "code": "36351005",
            "display": "Antithrombin III deficiency (disorder)"
          },
          {
            "code": "306058006",
            "display": "Aplastic anemia (disorder)"
          },
          {
            "code": "707147002",
            "display": "Asplenia (disorder)"
          },
          {
            "code": "65959000",
            "display": "Beta thalassemia (disorder)"
          },
          {
            "code": "64779008",
            "display": "Blood coagulation disorder (disorder)"
          },
          {
            "code": "715559004",
            "display": "Combined deficiency of factor V and factor VIII (disorder)"
          },
          {
            "code": "767712006",
            "display": "Factor IX deficiency (disorder)"
          },
          {
            "code": "4320005",
            "display": "Factor V deficiency (disorder)"
          },
          {
            "code": "307091009",
            "display": "Factor V Leiden mutation (disorder)"
          },
          {
            "code": "37193007",
            "display": "Factor VII deficiency (disorder)"
          },
          {
            "code": "76642003",
            "display": "Factor X deficiency (disorder)"
          },
          {
            "code": "767713001",
            "display": "Factor XI deficiency (disorder)"
          },
          {
            "code": "359727008",
            "display": "Fibrinogen deficiency (disorder)"
          },
          {
            "code": "90935002",
            "display": "Hemophilia (disorder)"
          },
          {
            "code": "41788008",
            "display": "Hereditary factor IX deficiency disease (disorder)"
          },
          {
            "code": "28293008",
            "display": "Hereditary factor VIII deficiency disease (disorder)"
          },
          {
            "code": "49762007",
            "display": "Hereditary factor XI deficiency disease (disorder)"
          },
          {
            "code": "84828003",
            "display": "Leukopenia (disorder)"
          },
          {
            "code": "109995007",
            "display": "Myelodysplastic syndrome (disorder)"
          },
          {
            "code": "165517008",
            "display": "Neutropenia (finding)"
          },
          {
            "code": "127034005",
            "display": "Pancytopenia (disorder)"
          },
          {
            "code": "109992005",
            "display": "Polycythemia vera (disorder)"
          },
          {
            "code": "76407009",
            "display": "Protein C deficiency disease (disorder)"
          },
          {
            "code": "1563006",
            "display": "Protein S deficiency disease (disorder)"
          },
          {
            "code": "440989002",
            "display": "Prothrombin G20210A mutation (disorder)"
          },
          {
            "code": "127041004",
            "display": "Sickle cell-beta-thalassemia (disorder)"
          },
          {
            "code": "127040003",
            "display": "Sickle cell-hemoglobin SS disease (disorder)"
          },
          {
            "code": "417357006",
            "display": "Sickling disorder due to hemoglobin S (disorder)"
          },
          {
            "code": "302215000",
            "display": "Thrombocytopenic disorder (disorder)"
          },
          {
            "code": "128105004",
            "display": "von Willebrand disorder (disorder)"
          }
        ]
      }
    ]
  }
}